187 English-speaking jobs in Walloon Brabant

This role contributes to the design and delivery of a biologics manufacturing facility, ensuring compliance with regulatory and quality requirements. The Qualification and Validation Lead will define and represent qualification and validation requirements, review technical documentation, and support audits and regulatory interactions.

Upstream Biomanufacturing Process Expert needed for biologics manufacturing facility design and delivery. Expertise in cell culture, bioreactor operations, and media preparation required. Collaborate with global teams and technical experts to ensure efficient, scalable production. Bachelor's degree in biotechnology, bioprocess engineering, or related field required. Proven experience in biologics manufacturing and regulated environments. Fluent in English. Occasional travel to the United States may be required.

Downstream Biomanufacturing Process Expert needed for a biologics manufacturing project. Will represent manufacturing needs, translate operational requirements, and ensure the future facility is designed for safe, high-quality, and efficient production. Requires a degree in a relevant field, experience in biopharmaceutical operations, and strong knowledge of mammalian biopharmaceutical production. Fluent in English, occasional travel to the US may be required.

Local Supply Chain & Warehousing Lead will represent Internal Manufacturing throughout the design and delivery of a new biologics manufacturing facility in Georgia, USA. The role requires expertise in supply chain and warehousing operations, including planning, procurement, inventory management, storage, logistics, and distribution.

Process Automation Lead will design and deliver automation solutions for a future-ready biologics manufacturing facility. This role requires experience in industrial automation within biopharmaceutical environments and knowledge of automation systems, industrial IT, and digital manufacturing tools.

Senior Solution Data Architect needed to define and implement data solutions, ensuring alignment with Target Enterprise Architecture. Requires 3+ years of experience as a Data Architect with strong Azure data stack expertise (Databricks, Synapse, ADF, CosmosDB, Azure SQL, Azure API Management, Azure App Services, Azure Analysis Services). Fluent English required.

Ensures robust quality oversight of GxP-relevant digital systems, focusing on compliant implementation and control of computerized systems and data processes. Collaborates with QA teams, Clinical Operations, and stakeholders to ensure systems are fit-for-purpose, validated, and operated in accordance with regulatory expectations.

Financial Manager to lead finance function and contribute to strategic development. Oversee accounting, reporting, audits, tax compliance, cash flow, and risk management. Lead and develop finance team, drive process improvements and digitalization initiatives.

Financial Manager to lead finance function and contribute to strategic development. Oversee accounting, reporting, audits, tax compliance, cash flow, and risk management. Lead and develop finance team, drive process improvements and digitalization.

Financial Manager to lead finance function and contribute to strategic development. Oversee accounting, reporting, audits, tax compliance, cash flow, and risk management. Lead and develop finance team, drive process improvements and digitalization.

Leads end-to-end regulatory reporting for Finance, ensuring compliance with National Bank of Belgium (NBB) obligations. Oversees capital, liquidity, recovery planning, and orderly wind-down initiatives.

Leads and shapes end-to-end clinical supply strategy across development programs. Manages end-to-end supply chain setup, including inventory, budget, and planning. Collaborates with stakeholders to integrate supply strategy into key development decisions.

Provides advanced scientific expertise in the safety evaluation and risk management of oncology assets in clinical development. Leads the identification, assessment, and communication of safety risks to ensure robust benefit-risk profiles. Drives the evaluation and interpretation of safety data, including signal detection and assessment. Contributes to safety components of global regulatory submissions. Represents Safety Evaluation & Risk Management on Clinical Matrix and Project Teams. Communicates safety recommendations and emerging risks to senior governance committees.

Leads global labelling strategy and execution for assigned vaccines and infectious diseases assets. Manages a team of labelling professionals and collaborates with cross-functional partners to ensure compliant and patient-focused labelling. Translates clinical and safety data into clear labelling content and represents the portfolio in labelling governance bodies.

Leads clinical safety and pharmacovigilance strategy for oncology assets within Global Safety. Oversees review, interpretation, and communication of safety data, ensuring timely identification, escalation, and management of safety issues. Develops and implements safety strategies, policies, and processes. Mentors SERM colleagues in signal evaluation, risk management, and preparation of regulatory safety deliverables.

Leads and shapes end-to-end clinical supply strategy across development programs. Manages end-to-end supply chain setup, including inventory, budget, and planning. Collaborates with stakeholders to integrate supply strategy into key development decisions.

The SERM Scientific Director provides in-depth medical/scientific expertise in the safety evaluation and risk management of GSK assets. This individual ensures scientifically sound review and interpretation of data, manages safety issues, and recommends further characterization, management, and communication of safety risks. Responsibilities include leading pharmacovigilance and risk management planning, leading the safety component of global regulatory submissions, and representing GSK on cross-functional teams.

Provides medical and scientific leadership in the safety evaluation and risk management of GSK's oncology assets in clinical development. Analyzes clinical data, literature, and emerging evidence to identify and assess safety signals. Leads pharmacovigilance and risk management activities for assigned oncology assets and clinical trials. Represents Safety on cross-functional Clinical Matrix and Project Teams. Communicates safety issues and recommendations to senior governance committees.

Offering and Pricing Lead role requires 8+ years of experience in pricing, commercial, or deal management within B2B SaaS or enterprise software. Must have a university degree in a related field and in-depth knowledge of SaaS pricing models, contract structures, and commercial best practices. Excellent communication, negotiation, and analytical skills are essential.

Provide technical support, configure software solutions, and analyze accounting needs for Belgian and Luxembourgish companies.